Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853426

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853426(-;-)
Make rs878853426(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112837908
GeneAPC
is asnp
is mentioned by
dbSNPrs878853426
ebirs878853426
HLIrs878853426
Exacrs878853426
Varsomers878853426
Maprs878853426
PheGenIrs878853426
hapmaprs878853426
1000 genomesrs878853426
hgdprs878853426
ensemblrs878853426
gopubmedrs878853426
geneviewrs878853426
scholarrs878853426
googlers878853426
pharmgkbrs878853426
gwascentralrs878853426
openSNPrs878853426
23andMers878853426
23andMe allrs878853426
SNP Nexus

SNPshotrs878853426
SNPdbers878853426
MSV3drs878853426
GWAS Ctlgrs878853426
Max Magnitude0
ClinVar
Risk rs878853426(;)
Alt rs878853426(;)
Reference rs878853426(A;A)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112173605delA
CLNSRC
CLNACC RCV000234542.1,